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US9809641B2ActiveUtilityPatentIndex 69

Lactoferrin fusion protein and method for preparation thereof

Assignee: NRL PHARMA INCPriority: Apr 23, 2012Filed: Apr 23, 2013Granted: Nov 7, 2017
Est. expiryApr 23, 2032(~5.8 yrs left)· nominal 20-yr term from priority
Inventors:SATO ATSUSHIKAGAYA SHINJI
A61P 9/12A61P 3/10A61P 35/04A61P 3/06A61P 7/06A61P 37/02A61P 43/00A61P 3/00A61P 25/08A61P 25/28A61P 25/22A61P 25/24A61P 29/00A61P 35/00A61P 31/12A61P 31/04A61P 25/04A61P 25/20A61P 25/16A61P 15/12A61P 13/08A61P 19/02A61P 25/00A61P 1/10A61P 1/16A61P 13/02A61P 1/02A61P 1/00A61K 38/00C07K 2319/30A01K 2217/052C07K 14/79A01K 67/0275A61K 38/40A01K 2267/01C12N 15/8241C12N 15/8257C12N 15/62
69
PatentIndex Score
3
Cited by
40
References
6
Claims

Abstract

The present invention aims to provide a lactoferrin fusion protein, which is configured to retain the biological activities of natural lactoferrin, to have a significantly prolonged in vivo lifetime, and to be more clinically useful than natural and gene recombinant lactoferrin, as well as a method for preparation thereof, etc. The present invention provides a fusion protein formed with a protein or peptide comprising an FcRn-binding region and lactoferrin or a biologically active fragment or peptide of lactoferrin, which is represented by: (LF- s -Y) n or (Y- s -LF) n [wherein LF represents lactoferrin or a biologically active fragment or peptide of lactoferrin, represents the protein or peptide comprising an FcRn-binding region, s represents ally amino acid sequence of 0 to 10 residues, and n represents an integer of 1 to 10], or a variant thereof.

Claims

exact text as granted — not AI-modified
The invention claimed is: 
     
       1. A fusion protein comprising the amino acid sequence of SEQ ID NO: 5 or 6. 
     
     
       2. A nucleic acid molecule encoding the fusion protein according to  claim 1 . 
     
     
       3. An expression vector comprising the nucleic acid molecule: according to  claim 2 . 
     
     
       4. An isolated host cell comprising the expression vector according to  claim 3 . 
     
     
       5. A pharmaceutical composition comprising the fusion protein according to  claim 1  and a carrier. 
     
     
       6. A method for preparing a fusion protein, which comprises culturing a host cell comprising the nucleic acid molecule of  claim 2  in a medium to express the fusion protein, and collecting the fusion protein from the host cell or the medium.

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